AR097199A1 - Inhibidores de rorc2 y sus métodos de uso - Google Patents
Inhibidores de rorc2 y sus métodos de usoInfo
- Publication number
- AR097199A1 AR097199A1 ARP140102904A ARP140102904A AR097199A1 AR 097199 A1 AR097199 A1 AR 097199A1 AR P140102904 A ARP140102904 A AR P140102904A AR P140102904 A ARP140102904 A AR P140102904A AR 097199 A1 AR097199 A1 AR 097199A1
- Authority
- AR
- Argentina
- Prior art keywords
- 4alkyl
- ch2c
- group
- 6alkyl
- independently selected
- Prior art date
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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Abstract
Compuestos, composiciones farmacéuticas, métodos para inhibir la actividad de RORg y/o reducir la cantidad de IL-17 en un sujeto, y métodos para tratar los diversos trastornos médicos usando estos compuestos y composiciones farmacéuticas. Compuestos útiles para tratar trastornos inflamatorios e inmunitorios. Reivindicación 1: Un compuesto caracterizado por las fórmulas (1), (2), (3), (4), (5), (6) ó (7), o una sal aceptable desde el punto de vista farmacéutico, un metabolito farmacéuticamente activo, un profármaco aceptable desde el punto de vista farmacéutico o un solvato de aquel aceptable desde el punto de vista farmacéutico, en donde, Y es hidrógeno, halo, ciano, C₁₋₃alquilo, C₁₋₃hidroxialquilo, C₁₋₅alquenilo, C₁₋₃haloalquilo, C₁₋₃hidroxihaloalquilo, C₃₋₆cicloalquilo, C₁₋₃alcoxi o C₁₋₃haloalcoxi; R¹ es hidrógeno, C₁₋₆alquilo, C₁₋₆hidroxialquilo o C₁₋₆haloalquilo; X es un compuesto seleccionado del grupo de fórmulas (8); R² es C₁₋₆alquilo, C₃₋₈cicloalquilo, C₃₋₈heterocicloalquilo, arilo o heteroarilo, sustituido opcionalmente con 1, 2, 3, 4 ó 5 sustituyentes seleccionados independientemente, para cada caso, del grupo que consiste en halo, ciano, C₁₋₄alquilo, C₁₋₄haloalquilo, C₁₋₄cianoalquilo, hidroxilo, -OR, C₁₋₄hidroxialquilo, C₁₋₄hidroxialcoxi, C₁₋₄hidroxialcoxiC₁₋₄alquilo, C₁₋₄alcoxi, C₁₋₄alcoxiC₁₋₄alquilo, C₁₋₄alcoxiC₁₋₄alcoxi, C₁₋₄alcoxiC₁₋₄alcoxiC₁₋₄alquilo, C₁₋₄haloalcoxi, -NR₂, (R₂N)C₁₋₄alquil-, C₁₋₄alquiltio, C₁₋₄haloalquiltio, -C(=O)R, -C(=O)OR, -OC(=O)R, -C(=O)NR₂, -N(R)C(=O)R, -CH₂C(=O)R, -CH₂C(=O)OR, -CH₂OC(=O)R, -CH₂C(=O)NR₂, -CH₂N(R)C(=O)R, -S(=O)₂R, -S(=O)₂NR₂, -N(R)S(=O)₂R, -A y -CH₂A; R se selecciona independientemente, para cada caso, del grupo que consiste en hidrógeno, C₁₋₄alquilo, C₁₋₄haloalquilo, C₁₋₄cianoalquilo, C₁₋₄hidroxialquilo, C₃₋₈cicloalquilo o C₃₋₈heterocicloalquilo; o en donde un nitrógeno se sustituye con dos grupos R, que se pueden tomar juntos con el átomo de nitrógeno al cual están unidos para formar un C₃₋₈heterocicloalquilo saturado de 4, 5, 6 ó 7 miembros que, cuando se forma, se puede sustituir opcionalmente con 1, 2 ó 3 sustituyentes seleccionados independientemente del grupo que consiste en C₁₋₄alquilo, halo, hidroxilo, C₁₋₄hidroxialquilo, C₁₋₄cianoalquilo, C₁₋₄haloalquilo y =O; A se selecciona independientemente, para cada caso, del grupo que consiste en C₃₋₈cicloalquilo, C₃₋₈heterocicloalquilo, arilo y heteroarilo, sustituido opcionalmente con 1, 2, 3, 4 ó 5 sustituyentes seleccionados independientemente, para cada caso, del grupo que consiste en halo, ciano, C₁₋₄alquilo, C₁₋₄haloalquilo, C₁₋₄cianoalquilo, hidroxilo, C₁₋₄hidroxialquilo, C₁₋₄alcoxi, C₁₋₄alcoxiC₁₋₄alquilo, C₁₋₄haloalcoxi, -NR₂, (R₂N)C₁₋₄alquil-, C₁₋₄alquiltio, C₁₋₄haloalquiltio, -C(=O)R, -C(=O)OR, -OC(=O)R, -C(=O)NR₂, -N(R)C(=O)R, -CH₂C(=O)R, -CH₂C(=O)OR, -CH₂OC(=O)R, -CH₂C(=O)NR₂, -CH₂N(R)C(=O)R, -S(=O)₂R, -S(=O)₂NR₂ y -N(R)S(=O)₂R; W es un resto seleccionado del grupo de fórmulas (9), sustituido opcionalmente con 1, 2, 3, 4 ó 5 sustituyentes seleccionados independientemente, para cada caso, del grupo que consiste en halo, C₁₋₆alquilo, C₁₋₆hidroxialquilo y C₁₋₆haloalquilo; R³ es C₁₋₆alquilo, C₃₋₈cicloalquilo, C₃₋₈heterocicloalquilo, arilo, heteroarilo, -C(=O)R⁴, -C(=O)OR⁴, -C(=O)N(R⁵)₂ o -S(=O)₂R⁴, sustituido opcionalmente con 1, 2, 3, 4 ó 5 sustituyentes seleccionados independientemente, para cada caso, del grupo que consiste en halo, ciano, C₁₋₄alquilo, C₁₋₄haloalquilo, C₁₋₄cianoalquilo, hidroxilo, C₁₋₄hidroxialquilo, C₁₋₄alcoxi, C₁₋₄alcoxiC₁₋₄alquilo, C₁₋₄haloalcoxi, -NR₂, (R₂N)C₁₋₄alquil-, C₁₋₄alquiltio, C₁₋₄haloalquiltio, -C(=O)R, -C(=O)OR, -OC(=O)R, -C(=O)NR₂, -N(R)C(=O)R, -CH₂C(=O)R, -CH₂C(=O)OR, -CH₂OC(=O)R, -CH₂C(=O)NR₂, -CH₂N(R)C(=O)R, -S(=O)₂R, -S(=O)₂NR₂, -N(R)S(=O)₂R, -A y-CH₂A; R⁴ es hidrógeno, C₁₋₆alquilo, C₃₋₈cicloalquilo, C₃₋₈heterocicloalquilo, C₃₋₈cicloalquilC₁₋₆alquilo, C₃₋₈heterocicloalquilC₁₋₆alquilo, arilo o heteroarilo, sustituido opcionalmente con 1, 2, 3, 4 ó 5 sustituyentes seleccionados independientemente, para cada caso, del grupo que consiste en halo, ciano, C₁₋₄alquilo, C₁₋₄haloalquilo, C₁₋₄cianoalquilo, hidroxilo, C₁₋₄hidroxialquilo, C₁₋₄alcoxi, C₁₋₆alcoxiC₁₋₆alquilo, C₁₋₆haloalcoxi, -NR₂, (R₂N)C₁₋₆alquilo, C₁₋₆alquiltio, C₁₋₆haloalquiltio, -C(=O)R, -C(=O)OR, -OC(=O)R, -C(=O)NR₂, -N(R)C(=O)R, -CH₂C(=O)R, -CH₂C(=O)OR, -CH₂OC(=O)R, -CH₂C(=O)NR₂, -CH₂N(R)C(=O)R, -S(=O)₂R, -S(=O)₂NR₂, -N(R)S(=O)₂R, -A Y -CH₂A; y R⁵ se selecciona independientemente, para cada caso, del grupo que consiste en hidrógeno, C₁₋₆alquilo, C₃₋₈cicloalquilo, C₃₋₈heterocicloalquilo, C₃₋₈cicloalquilC₁₋₆alquilo, C₃₋₈heterocicloalquilC₁₋₆alquilo, arilo y heteroarilo, sustituido opcionalmente con 1, 2, 3, 4 ó 5 sustituyentes, seleccionados independientemente, para cada caso, del grupo que consiste en halo, ciano, C₁₋₄alquilo, C₁₋₄haloalquilo, C₁₋₄cianoalquilo, hidroxilo, C₁₋₄hidroxialquilo, C₁₋₄alcoxi, C₁₋₄alcoxiC₁₋₄alquilo, C₁₋₄haloalcoxi, -NR₂, (R₂N)C₁₋₄alquil-, C₁₋₄alquiltio, C₁₋₄haloalquiltio, -C(=O)R, -C(=O)OR, -OC(=O)R, -C(=O)NR₂, -N(R)C(=O)R, -CH₂C(=O)R, -CH₂C(=O)OR, -CH₂OC(=O)R, -CH₂C(=O)NR₂, -CH₂N(R)C(=O)R, -S(=O)₂R, -S(=O)₂NR₂, -N(R)S(=O)₂R, -A y -CH₂A; o en donde un nitrógeno se sustituye con dos grupos R⁵ que pueden tomarse junto el átomo de nitrógeno al que están unidos para formar un C₃₋₈ heterocicloalquilo saturado de 4, 5, 6 ó 7 miembros que, cuando se forma, se puede sustituir opcionalmente con 1, 2 ó 3 sustituyentes seleccionados independientemente del grupo que consiste en C₁₋₄alquilo, halo, hidroxilo, C₁₋₄hidroxialquilo, C₁₋₄haloalquilo y =O.
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| MA40759A (fr) * | 2014-09-26 | 2017-08-01 | Pfizer | Modulateurs de rorc2 de type pyrrolopyridine substitué par un méthyle et trifluorométhyle et leurs procédés d'utilisation |
| CA2975157C (en) | 2015-01-30 | 2019-09-17 | Pfizer Inc. | Sulfonamide-substituted indole modulators of rorc2 and methods of use thereof |
| US10336748B2 (en) * | 2015-01-30 | 2019-07-02 | Pfizer Inc. | Methyoxy-substituted pyrrolopyridine modulators of RORC2 and methods of use thereof |
| CN104672121B (zh) * | 2015-02-16 | 2017-10-24 | 上海华默西医药科技有限公司 | 2r‑(2,5‑二氟苯基)吡咯烷盐酸盐的制备方法 |
| HRP20200064T1 (hr) * | 2015-06-09 | 2020-04-03 | Abbvie Inc. | Modulatori nuklearnih receptora (ror) namijenjeni liječenju upalnih i autoimunih bolesti |
| EP3558363A1 (en) | 2016-12-21 | 2019-10-30 | Amgen Inc. | Anti-tnf alpha antibody formulations |
| GB201709456D0 (en) * | 2017-06-14 | 2017-07-26 | Ucb Biopharma Sprl | Therapeutic agents |
| CN109206401B (zh) * | 2017-06-29 | 2021-03-05 | 南京柯菲平盛辉制药有限公司 | 一类甲基-1H-吲唑类RORγ调节剂及其用途 |
| JP6557436B1 (ja) * | 2018-03-12 | 2019-08-07 | アッヴィ・インコーポレイテッド | チロシンキナーゼ2媒介性シグナル伝達の阻害剤 |
| WO2021007477A1 (en) | 2019-07-11 | 2021-01-14 | E-Scape Bio, Inc. | Indazoles and azaindazoles as lrrk2 inhibitors |
| CN112745268B (zh) * | 2019-10-31 | 2022-09-16 | 江苏恒瑞医药股份有限公司 | 苯并咪唑衍生物的晶型及制备方法 |
| WO2021209377A1 (en) * | 2020-04-16 | 2021-10-21 | Basf Se | A process for the preparation of 4-cyanobenzoyl chlorides |
| CN119119032B (zh) * | 2024-08-05 | 2025-09-09 | 中山大学附属第三医院 | 一种吲哚苯甲酰胺类衍生物及其制备方法和应用 |
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